Labeled d8 Desmethyl Clozapine Hydrochloride
Labeled d8 Desmethyl Clozapine Hydrochloride Basic information
- Product Name:
- Labeled d8 Desmethyl Clozapine Hydrochloride
- Synonyms:
-
- Labeled d8 Desmethyl Clozapine Hydrochloride
- N-DESMETHYLCLOZAPINE (D8, 98%) 100 UG/ML IN METHANOL
- [2H8]-N-Desmethyl Clozapine
- 6-chloro-10-[(2,2,3,3,5,5,6,6-2H?)piperazin-1-yl]-2,9-diazatricyclo[9.4.0.03,?]pentadeca-1(11),3(8),4,6,9,12,14-heptaene
- N-Desmethylclozapine-D8 solution
- D8-N-Desmethyl Clozapine
- CAS:
- 1189888-77-4
- MF:
- C17H17ClN4
- MW:
- 312.8
- Mol File:
- 1189888-77-4.mol
Labeled d8 Desmethyl Clozapine Hydrochloride Chemical Properties
- storage temp.
- Store at -20°C
- solubility
- DMF: 10 mg/ml,DMSO: 10 mg/ml,DMSO:PBS (pH 7.2) (1:1): 0.5 mg/ml,Ethanol: 5 mg/ml
- form
- A solid
- color
- White to off-white
- Major Application
- clinical testing
Labeled d8 Desmethyl Clozapine Hydrochloride Usage And Synthesis
Uses
A major labelled metabolite of clozapine. A potent and selective 5-HT2C serotonin receptor antogonist.
Biological Activity
N-Desmethylclozapine-d8 is intended for use as an internal standard for the quantification of N-desmethylclozapine by GC- or LC-MS. N-Desmethylclozapine is an active metabolite of the atypical antipsychotic clozapine .1 It was originally described as an antagonist of serotonin (5-HT) receptor subtype 5-HT2C (IC50 = 7.1 nM in rat choroid plexus) and later as an inverse agonist using human recombinant receptors.2,3 N-Desmethylclozapine is an antagonist at dopamine D4 receptors, an agonist at δ-opioid receptors, and a partial agonist at dopamine D2 and D3, M1 muscarinic acetylcholine, and 5-HT1A receptors.3,1,4 N-Desmethylclozapine (30 mg/kg) decreases exploratory locomotor activity and increases prepulse inhibiton of the acoustic startle response in mice.5
IC 50
mAChR1; δ Opioid Receptor/DOR
References
1.Burstein, E.S., Ma, J., Wong, S., et al.Intrinsic efficacy of antipsychotics at human D2, D3, and D4 dopamine receptors: Identification of the clozapine metabolite N-desmethylclozapine as a D2/D3 partial agonistJ. Pharmacol. Exp. Ther.315(3)1278-1287(2005) 2.Kuoppam?ki, M., Syv?lahti, E., and Hietala, J.Clozapine and N-desmethylclozapine are potent 5-HT1C receptor antagonistsEur. J. Pharmacol.245(2)179-182(1993) 3.Lameh, J., Burstein, E.S., Taylor, E., et al.Pharmacology of N-desmethylclozapinePharmacol. Ther.115(2)223-231(2007) 4.Odagaki, Y., Kinoshita, M., and Ota, T.Comparative analysis of pharmacological properties of xanomeline and N-desmethylclozapine in rat brain membranesJ. Psychopharmacol.30(9)896-912(2016) 5.Maehara, S., Hikichi, H., and Ohta, H.Behavioral effects of N-desmethylclozapine on locomotor activity and sensorimotor gating function in mice-Possible involvement of muscarinic receptorsBrain Res.1418111-119(2011)
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